HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632284Generated: November 2, 2026
N-Benzoylcytidine → HCID 178418385, compound
https://huagongshe.com/reaction/1632284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Benzoylcytidine | HCID 10066259 | — |
| Reactant | HCID 178420932 | HCID 178420932 | — |
| Reactant | HCID 178527074 | HCID 178527074 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178418385 | HCID 178418385 | — |
| Product | HCID 178418441 | HCID 178418441 | — |
Reaction Steps
N-Benzoylcytidine linked from the 3' hydroxyl group via a hemisuccinate bridge to aminopropyl-substituted HPLC-grade silica (Vydac) was used as the solid-phase support. Samples (100 mg each; 10 micromoles) were shaken in sealed test tubes in acetonitrile (1 ml) with each of the four 5'-dimethoxytrityl-deoxynucleoside-3'-dimethylaminophosphoramidites and either tetrazole (1 mmole) or benzotriazole (600 micromoles) to form the tetrazolide or benzotriazolide-phosphite active species, the latter being a compound of this invention. After thorough washing by repeated centrifugation and subsequent decanting, and oxidation with 0.01M iodine, the support was treated with 2.75% (w/v) trichloroacetic acid in methylene chloride (10 ml) for 5 minutes. Spectrophotometric assay of the dimethoxytrityl carbonium ion produced in the supernatant demonstrated that all couplings had proceeded to greater than 95% of theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04474948 |
|---|
| Source dataset | uspto-grants-1984_10 |
|---|
| ORD ID | ord-a7da0d4ca9bf4f2bab299c45fcc0c396 |
|---|
| Source note | uspto-grants-1984_10 |
|---|